HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2,4-Dichlorobenzoyl Cyanide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2,4-Dichlorobenzoyl chloride | HCID 66645 | — |
| Product | 2,4-Dichlorobenzoyl Cyanide | HCID 9834232 | — |
Reaction Steps
The reaction was carried out under Argon. Cuprous cyanide (5.0 g, 56.0 mmol) and anhydrous sodium iodide (15.6 g, 104 mmol) were stirred for 2 minutes in anhydrous acetonitrile (100 ml). The resulting solution was mixed with 2,4-dichlorobenzoyl chloride (10.96 g, 52.3 mmol) whereupon an orange precipitate formed. The mixture was stirred for 30 minutes at room temperature, filtered and concentrated in vacuo. The residue was taken up in dichloromethane and the resulting precipitate was filtered off. Concentration of the filtrate under reduce pressure gave a yellow solid which was recrystallised from 60°-80° C. b.p.t. petroleum ether to give 2,4-dichlorobenzoyl cyanide as cream coloured crystals (8.36 g, 80%), melting point 73°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210312 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-bd6ce932a1a2450ebfed5f074f38155a |
| Source note | uspto-grants-1993_05 |